项目名称: 美洲大蠊提取液对大鼠难愈合创面TGF-β1/Smads通路、ECM及DED的调控研究
项目编号: No.81503585
项目类型: 青年科学基金项目
立项/批准年度: 2016
项目学科: 医药、卫生
项目作者: 曾娟妮
作者单位: 湖南中医药大学
项目金额: 18万元
中文摘要: 体表慢性难愈合创面 (俗称皮肤溃疡)已成为危害人类健康的公共问题,目前临床上仍缺乏有效简廉的治疗方法。最新研究表明,TGF-β1/Smads信号通路在难愈合创面的愈合过程中发挥着相当重要的作用,而生长因子调节细胞外基质的合成与降解以及细胞增殖与凋亡是伤口愈合的关键。课题组前期研究发现美洲大蠊提取液能促进难愈合创面愈合,并能提高组织中VEGFmRNA的表达,但促愈机制尚未完全清楚。此项目在前期研究的基础上,分别运用电镜技术、Western Blot、Real-time PCR、免疫组化等方法,研究美洲大蠊提取液对慢性难愈合创面愈合过程中有关细胞外基质及细胞凋亡等的蛋白和基因表达的调控,以期从TGF-β1/Smads信号通路、ECM及细胞凋亡角度,进一步阐明美洲大蠊提取液促进慢性难愈合创面修复的分子机制,为临床推广应用美洲大蠊提取液防治慢性难愈合创面提供一种可靠的治疗方法和理论依据。
中文关键词: 美洲大蠊提取液;慢性难愈合创面;TGF-β1/Smads信号通路;细胞外基质;细胞凋亡
英文摘要: Chronic nonhealing wound, known as skin ulcer, has been become one of the public health problems, and there is no effective, simple and inexpensive treatment for this disease in clinical practice at the present. The lastest studies indicated that the TGF-β1/Smads signaling pathway plays the important role in wound healing process,and growth factors regulate the synthesis and degradation of extracellular matrix and cell proliferation and apoptosis are the key to wound healing. Our previous study found that Periplaneta Americana extract can promote chronic nonhealing wound repair and enhance the expression of VEGFmRNA on tissue, but the mechanism is not completely understood. This project, based on previous studies, aims to research the Periplaneta Americana extract regulate ECM and cell apoptosis on the expression of proteins or genes during the process of chronic nonhealing wound healing in rats by use of the electron microscopy, the Western Blot, the Real-time PCR,the Immunohistochemistry and so on. which will further illuminate the molecular mechanism of the Periplaneta Americana extract in promoting chronic nonhealing wound repair based on the TGF-β1/Smads signaling pathway, ECM and cell apoptosis, and provide a reliable treatment method and theoretical basis for clinical application periplaneta Americana extract to prevent and treat the chronic nonhealing wound.
英文关键词: Periplaneta Americana extract ;chronic nonhealing wound;TGF-β1/Smads signaling pathway ;ECM;DED